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Sandy
- Female
- Pepperell, MA
- United States
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Latest Activity
Sandy left a comment for Cindy and Samantha"Hi Cindy and Samantha,
She has her good days and bad days. She is 16 so it's a tough age anyway. Her spots are growing back in. I am going to start her on vitamin D. Autoimmune disease has alot to do with a lack of sun and vitamin D. I'll…"
Sandy replied to Angie Simonet's discussion Advice for a heartbroken mom"Hi Suzi,
I saw your comment about this Dr. Rohit. I have to say i am excited about what you said. Are you still useing this treatment. My daughter is 16 and was diognosed with AA back in september 2009. do you really recommend this. How fast did it…"
Cindy and Samantha left a comment for Sandy"Hi Sandra, I am in Mass too and I have an 8 yr old daughter. I also do a support group through the Children's Alopecia Project. We meet at Newton Wellsely Hospital bi monthly.
Please don't by the Calosol. I got sucked into it with no…"
Sandy replied to Jen Deletto's discussion Wigs for Kids"Hi Jen I am Sandra and new to the website. I have a 16 year old daughter diognosed with AA back in September. a couple of days ago I got on a site called locksoflove. I had been familiar with this locksoflove because I have a friend that donates his…"
Profile Information
- Relationship Status:
- Married
- About Me:
- Have a 18year old daughter suffering from alopecia areata for 2 years now. Have found some help. Locks of Love does give real hair wigs for people that suffer from alopecia under age 21
- Do you have alopecia?
- Parent or guardian of child with alopecia
- Are you age 18 or older?
- Yes - I am 18 or older
Sandy's Photos
Comment Wall (6 comments)
- At 2:44pm on March 21, 2010,
Rose Marie' said… - Hi
Just noticed you have a daughter with alopecia - I do as well. If I can of any support or help just drop me a line.
(I have my page set to private so I will put in a friend request for you).
I'll look forward to getting to know you.
Rosy
- At 10:24am on March 21, 2010, Cindy and Samantha said…
- Please feel free to contact me anytime.
- At 1:45pm on March 19, 2010, Cindy and Samantha said…
- Hi Sandra, I am in Mass too and I have an 8 yr old daughter. I also do a support group through the Children's Alopecia Project. We meet at Newton Wellsely Hospital bi monthly.
Please don't by the Calosol. I got sucked into it with no results and it is a scam. Please contact me privately if you would like to talk about it. I am also happy to give you a good pediatric derm to see at Children's Hosptial. How is your daughter handling it all? Cindy
- At 4:18pm on March 17, 2010,
LeslieAnn Butler said…
- I know how hard it can be. And you want to fix it, but you can't.
My book, "If Your Hair Falls Out, Keep Dancing!" has helped a lot of people -- you might want to get it (on Amazon). You can find out more about it on my page and it has good reviews on Amazon.
Meanwhile, I am here for support and advice.
- At 7:09pm on March 16, 2010,
- Hello and welcome, Sandra!
How are you and your daughter doing today?
Be careful of products like Calosol. There's really no cure for alopecia at this time, although researchers are working on it!
LeslieAnn
- At 2:04am on March 16, 2010,
Dotty said… - Welcome to Alopecia World,
I live in NH but am originally from MA. If you need anything at all, let me know. This is a wonderful place to meet new friends and find lots of support. I have an Alopecia non-profit and we try to plan get togethers in the MA/NH area. I will keep you updated if you would like of the next planned meeting. Hope you take advantage of the support here.
Love and Hugs,
Dotty
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